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Azadegan-Dehkordi, F and Bahrami, T and Shirzad, M and Karbasi, G and Yazdanpanahi, N and Farrokhi, E and Koohiyan, M and Tabatabaiefar, M and Hashemzadeh-Chaleshtori, M (2018) Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran. J Audiol Otol.
Azadegan-Dehkordi, F and Ahmadi, R and Koohiyan, M and Hashemzadeh-Chaleshtori, M (2018) Update of spectrum c.35delG and c.-23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss. Ann Hum Genet.
Azadegan-Dehkordi, F and Ahmadi, R and Bahrami, T and Yazdanpanahi, N and Farrokhi, E and Tabatabaiefar, MA and Hashemzadeh-Chaleshtori, mahmoud (2018) A novel variant of SLC26A4 and first report of the c.716T>A variant in Iranian pedigrees with non-syndromic sensorineural hearing loss. Am J Otolaryngol.
